Registration number (WIID)Project No.TitleStatus
32001LVS EN ISO 10993-15:2009Biological evaluation of medical devices - Part 15: Identification and quantification of degradation products from metals and alloys (ISO 10993-15:2000)Atcelts
40815LVS EN ISO 10993-4:2017Biological evaluation of medical devices - Part 4: Selection of tests for interactions with blood (ISO 10993-4:2017)Atcelts
27092LVS EN ISO 10993-1:2010Biological evaluation of medical devices - Part 1: Evaluation and testing within a risk management process (ISO 10993-1:2009)Atcelts
9489LVS EN ISO 10993-15:2003Biological evaluation of medical devices - Part 15: Identification and quantification of degradation products from metals and alloysAtcelts
9475LVS EN 30993-3:1993Biological evalution of medical devices - Part 3: Tests for genotoxicity, carcinogenicity and reproductive toxicityAtcelts
27092EN ISO 10993-1:2009Biological evaluation of medical devices - Part 1: Evaluation and testing within a risk management system (ISO/FDIS 10993-1:2009)Atcelts
32007EN ISO 10993-11:2009Biological evaluation of medical devices - Part 11: Tests for systemic toxicity (ISO 10993-11:2006)Atcelts
9477EN ISO 10993-10:1995Biological evaluation of medical devices - Part 10: Tests for irritation and sensitization (ISO 10993-10:1995)Atcelts
9480EN 30993-6:1994Biological evaluation of medical devices - Part 6: Tests for local effects after implantation (ISO 10993-6:1994)Atcelts
9481EN ISO 10993-7:1995Biological evaluation of medical devices - Part 7: Ethylene oxide sterilization residuals (ISO 10993-7:1995)Atcelts
Displaying 101-110 of 190 results.